Evidence map›Paper›PMID 35609865›Full record

ArticleTransplantation and cellular therapy2022

Outcomes of Autologous Hematopoietic Cell Transplantation in Older Patients with Diffuse Large B-Cell Lymphoma.

Pashna N Munshi, Yue Chen, Kwang W Ahn, Farrukh T Awan, Amanda Cashen, Geoffrey Shouse, Mazyar Shadman, Paul Shaughnessy, Joanna Zurko, Frederick L Locke and 8 more

Open access · greenAbstract read
In one paragraph

Article in Transplantation and cellular therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 14 institutions in 1 country.

Pashna N MunshiMedStar Georgetown University Hospital, Stem Cell Transplant and Cellular Immunotherapy Program, Division of Hematology & Oncology, Washington, District of Columbia.
Yue ChenCIBMTR (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Kwang W AhnCIBMTR (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin; CIBMTR, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI Division of Biostatistics, Institute for Health and Equity, Medical College of Wisconsin, Milwaukee, Wisconsin.
Farrukh T AwanDivision of Hematology/Oncology, UT Southwestern Medical Center, Dallas, Texas.
Amanda CashenWashington University School of Medicine, Department of Medicine, Division of Medical Oncology, St. Louis, Missouri.
Geoffrey ShouseDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, City of Hope, California.
Mazyar ShadmanClinical Research Division, Fred Hutchinson Cancer Research Center and Medical Oncology division, Department of Medicine, University of Washington, Seattle, Washington.
Paul ShaughnessySarah Cannon Transplant and Cellular Therapy Program, Methodist Hospital, San Antonio, Texas.
Joanna ZurkoDivision of Hematology & Oncology, Medical College of Wisconsin, Milwaukee, Wisconsin.
Frederick L LockeDepartment of Blood and Marrow Transplant and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, Florida.
Aaron M GoodmanDivision of Blood and Marrow Transplantation, University of California San Diego, San Diego, California.
Jose C Villaboas BisnetoDepartment of Medicine, Division of Hematology, Mayo Clinic, Rochester, Minnesota.
Craig SauterDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, N.Y.; Department of Medicine, Weill Cornell Medical College, New York, New York.
Mohamad A Kharfan-DabajaBlood and Marrow Transplantation and Cellular Therapies, Mayo Clinic, Jacksonville, Florida.
Gabrielle MeyersDepartment of Medicine, Division of Hematology and Oncology, Knight Cancer Institute, Oregon Health and Science University, Portland, Oregon.
Samantha JaglowskiDepartment of Internal Medicine, Division of Hematology and Oncology, Comprehensive Cancer Center at The Ohio State University, Columbus, Ohio.
Alex HerreraDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, City of Hope, California.
Mehdi HamadaniCIBMTR (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin; BMT & Cellular Therapy Program, Medical College of Wisconsin, Milwaukee, Wisconsin. Electronic address: mhamadani@mcw.edu.
Medical College of Wisconsin · USCity Of Hope National Medical Center · USGeorgetown University · USMayo Clinic · USMayo Clinic in Florida · USMemorial Sloan Kettering Cancer Center · USMoffitt Cancer Center · USOregon Health & Science University · USSarah Cannon · USSouthwestern Medical Center · USThe Ohio State University · USUniversity of California San Diego · USUniversity of Washington · USWashington University in St. Louis · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
NCI NIH HHS P30 CA008748NCI NIH HHS U24 CA076518
6 · The paper itself

Abstract

Data for outcomes after autologous hematopoietic cell transplantation (auto-HCT) in diffuse large B-cell lymphoma (DLBCL) patients ≥70 years are limited. Auto-HCT is feasible in older DLBCL patients. Using the Center for International Blood and Marrow Transplant Research database, we compared outcomes of auto-HCT in DLBCL patients aged 60 to 69 years (n = 363) versus ≥70 years (n = 103) between 2008 and 2019. Non-relapse mortality (NRM), relapse/progression (REL), progression-free survival (PFS), and overall survival (OS) were modeled using Cox proportional hazards models. All patients received BEAM conditioning (carmustine, etoposide, cytosine arabinoside and melphalan). On univariate analysis, in the 60 to 69 years versus ≥70 years cohorts, 100-day NRM was 3% versus 4%, 5-year REL was 47% versus 45%, 5-year PFS 40% versus 38% and 5-year OS 55% versus 41%, respectively. On multivariate analysis, patients ≥70 had no significant difference in NRM (hazard ratio [HR] 1.43, 95% confidence interval [CI] 0.85-2.39), REL (HR 1.11, 95% CI 0.79-1.56), PFS (HR 1.23, 95% CI 0.92-1.63) compared to patients 60 to 69 years. Patients ≥70 years had a higher mortality (HR 1.39, 95% CI 1.05-1.85, p=0.02), likely because of inferior post-relapse OS in this cohort (HR 1.82, 95% CI 1.27-2.61, P = .001). DLBCL was the major cause of death in both cohorts (62% versus 59%). Older patients should not be denied auto-HCT solely on the basis of chronological age.

Indexed as

Hematopoietic Stem Cell TransplantationLymphoma, Large B-Cell, DiffuseAgedHumansNeoplasm Recurrence, LocalTransplantation, AutologousTransplantation ConditioningAutologous transplantBEAMDiffuse large B cell lymphomaOlderRelapse

Identifiers

PMID35609865
PMCPMC9375438
OpenAlexW4281251441

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.